The mutation in Brems1 resulting in male sterility in Chinese cabbage were validated through two allelic mutations. Male sterile lines are ideal for hybrid seed production in Chinese cabbage. Herein, the complete male sterile mutants M5026 and M5073 were obtained through ethyl methanesulfonate (EMS) mutagenesis in the Chinese cabbage double haploid line 'FT'. Cytological observations revealed that M5026 exhibited an absence of the tapetum, an overabundance of microsporocytes, and abnormal exine formation in pollen. The male sterility phenotype of M5026 was controlled by a single recessive nuclear gene. Using mutmap sequencing and kompetitive allele-specific PCR (KASP) identification and gene cloning, two distinct SNPs in BraA10g029920.3.5C, encoding EMS1 (excess microsporocytes 1), were identified to be associated with the male sterility of M5026 and M5073. The gene was named as Brems1. M5026 and M5073 were determined to be allelic variants. Both BrEMS1 and Brems1 were subcellularly localized at the cell membrane. Brems1 exhibited the highest expression level in buds, while no expression was detected in roots. Transcriptomic analysis revealed that Brems1 mutations reduced the expression levels of genes associated with the tapetum, pollen tube, and LRR-RLK family. These results suggested that Brems1 played a critical role in pollen development and contributes to elucidating the molecular mechanisms underlying tapetum development and male sterility in Chinese cabbage.
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http://dx.doi.org/10.1007/s00122-025-04841-y | DOI Listing |
Andrology
March 2025
CIBB - Centre for Innovative Biomedicine and Biotechnology, University of Coimbra, Coimbra, Portugal.
Zhejiang Da Xue Xue Bao Yi Xue Ban
March 2025
Institute of Translational Medicine, Yangzhou University Medical College, Yangzhou 225009, Jiangsu Province, China.
Sertoli cells play an important role in the process of spermatogenesis by providing energy for spermatogenic cells and themselves through glycolysis and fatty acid oxidation. Abnormalities in spermatogenesis are closely related to disruptions of glucose and lipid metabolism in Sertoli cells. The metabolic environment of Sertoli cells is hypoxic, with glycolysis and fatty acid β-oxidation being the primary metabolic pathways.
View Article and Find Full Text PDFHum Fertil (Camb)
December 2025
Centre for Biostatistics, Manchester Academic Health Science Centre, Division of Population Health, Health Services Research and Primary Care, University of Manchester, Manchester, UK.
This study presents the findings from a UK-based survey exploring fertility treatment add-ons, treatment costs, and information transparency. The online survey, distributed via social media, targeted current and prospective IVF patients, yielding 304 eligible responses. Results indicate an increase in the use of fertility treatment add-ons compared to previous data.
View Article and Find Full Text PDFJ Assist Reprod Genet
March 2025
Department of Reproductive Medicine, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, 210002, Jiangsu, China.
Purpose: We aimed to demonstrate the genetic factors of primary gonadal dysgenesis in a consanguineous family characterized by underdeveloped testes and non-obstructive azoospermia (NOA) in a male and primary amenorrhoea and primary ovarian insufficiency (POI) in a female.
Methods: DNA was extracted from the male proband with infertility from the consanguineous family for whole-exome sequencing and bioinformatics analysis to screen for potential pathogenic genes and mutations. Sanger sequencing was used for further validation of his family pedigree.
Fertil Steril
March 2025
Dept. of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy; Department of Andrology, Fundació Puigvert, Universitat Autònoma de Barcelona, Instituto de Investigaciones Biomédicas Sant Pau (IIB-Sant Pau), Barcelona, Catalonia, Spain.
The crucial role of Y chromosome genes in male gonadal determination and reproductive fitness has been recognized for decades. Y chromosome microdeletions are the most common molecular genetic causes of azoospermia and severe spermatogenic impairment. Since the late 1990s, screening for these microdeletions has become a routine part of the diagnostic work-up of severe male factor infertility.
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